rs16860281

Homo sapiens
T>C
None
Check p-value
SNV (Single Nucleotide Variation)
C=0108 (3240/29962,GnomAD)
C=0132 (3871/29118,TOPMED)
C=0095 (474/5008,1000G)
C=0088 (341/3854,ALSPAC)
C=0091 (339/3708,TWINSUK)
chr3:148277560 (GRCh38.p7) (3q24)
ND
GWASdb2
1   publication(s)
See rs on genome
7 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 3NC_000003.12:g.148277560T>C
GRCh37.p13 chr 3NC_000003.11:g.147995347T>C

Genomic View

Chromatin Interaction

There is no significant Hi-C chromatin interaction data for this SNP.

Enhancer Annotation (GRCh37.p13)

Chromosome Start End Region Distance ( -/+ : Up/Downstream )
chr3147987063147988743E069-6604
chr3147987063147988743E071-6604
chr3147987063147988743E072-6604
chr3147947105147947165E074-48182
chr3147983419147983655E074-11692
chr3147983693147983967E074-11380
chr3147987063147988743E074-6604




Mpgyi